Quick quiz may spot alcohol risk in pregnancy without a blood test
NCT ID NCT04786587
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is checking whether a short self-report questionnaire called T-ACE can accurately identify pregnant women who drink alcohol at high-risk levels. About 2,425 pregnant women in three French hospitals will fill out the questionnaire and then give a blood sample to measure a biomarker of recent alcohol use. The goal is to see if the questionnaire is a reliable, non-invasive screening tool that could be used widely in prenatal care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If the T-ACE questionnaire proves accurate, it could become a standard, quick tool to identify pregnant women who may need help with alcohol use.
- What could go wrong
- This is a diagnostic study, not a treatment trial. The questionnaire may not be sensitive or specific enough to replace blood tests, and results may not apply outside the study hospitals.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,425 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Pregnant women followed in 3 maternity hospitals in the North of France
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * pregnant woman over 18 years old, presenting in one of the three maternities of the study for her prenatal care * and having returned her self-report * and having given her written consent * no exclusion criteria Exclusion Criteria: * woman under 18 years old * or not pregnant * or not having returned her self-report * or woman who refused to participate in the study (absence of written consent)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital, Lille
RECRUITINGLille, 59000, France
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